Lerner, Leon M. published an article in 1977, the title of the article was Enantiomeric forms of 9-(5-deoxy-β-erythro-pent-4-enofuranosyl)adenine and a new preparation of 5-deoxy-D-lyxose.Electric Literature of 38838-06-1 And the article contains the following content:
Tosylation of Me 2,3-O-isopropylidene-β-D-ribofuranoside followed by treatment with NaI, deisopropylidenation, benzoylation, and acetolysis gave I. Condensation of I with 6-benzamidochloromercuripurine followed by treatment with 1,5-diazabicyclo[5.4.0]undec-5-ene and subsequent deblocking gave II. The enantiomeric III was similarly prepared from Me 2,3-O-isopropylidene-α-D-lyxopyranoside (IV). Oxidation of Me 2,3-O-isopropylidene-α-D-mannofuranoside with NaIO4 followed by reduction with NaBH4 to give IV and subsequent acid hydrolysis gave D-lyxose. Tosylation of IV followed by reductive cleavage and subsequent hydrolysis gave 5-deoxy-D-lyxose. The experimental process involved the reaction of (3aS,4S,6R,6aR)-4-(Iodomethyl)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole(cas: 38838-06-1).Electric Literature of 38838-06-1
The Article related to adenine deoxypentenofuranosyl, pentenofuranosyl deoxy adenine, nucleoside dehydrodeoxy, lyxose deoxy, pentose deoxy, ribofuranose condensation benzamidopurine, purine benzamido condensation ribofuranose and other aspects.Electric Literature of 38838-06-1
Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem